217 related articles for article (PubMed ID: 35718780)
1. Novel copy number variations within SYCE1 caused meiotic arrest and non-obstructive azoospermia.
Huang Y; Tian R; Xu J; Ji Z; Zhang Y; Zhao L; Yang C; Li P; Zhi E; Bai H; Han S; Luo J; Zhao J; Zhang J; Zhou Z; Li Z; Yao C
BMC Med Genomics; 2022 Jun; 15(1):137. PubMed ID: 35718780
[TBL] [Abstract][Full Text] [Related]
2. Novel bi-allelic MSH4 variants causes meiotic arrest and non-obstructive azoospermia.
Li P; Ji Z; Zhi E; Zhang Y; Han S; Zhao L; Tian R; Chen H; Huang Y; Zhang J; Chen H; Zhao F; Zhou Z; Li Z; Yao C
Reprod Biol Endocrinol; 2022 Jan; 20(1):21. PubMed ID: 35090489
[TBL] [Abstract][Full Text] [Related]
3. Novel exon mutation in SYCE1 gene is associated with non-obstructive azoospermia.
Feng K; Ge H; Chen H; Cui C; Zhang S; Zhang C; Meng L; Guo H; Zhang L
J Cell Mol Med; 2022 Feb; 26(4):1245-1252. PubMed ID: 35023261
[TBL] [Abstract][Full Text] [Related]
4. Sequencing of a 'mouse azoospermia' gene panel in azoospermic men: identification of RNF212 and STAG3 mutations as novel genetic causes of meiotic arrest.
Riera-Escamilla A; Enguita-Marruedo A; Moreno-Mendoza D; Chianese C; Sleddens-Linkels E; Contini E; Benelli M; Natali A; Colpi GM; Ruiz-Castañé E; Maggi M; Baarends WM; Krausz C
Hum Reprod; 2019 Jun; 34(6):978-988. PubMed ID: 31125047
[TBL] [Abstract][Full Text] [Related]
5. Bi-allelic
Yao C; Yang C; Zhao L; Li P; Tian R; Chen H; Guo Y; Huang Y; Zhi E; Zhai J; Sun H; Zhang J; Hong Y; Zhang L; Ji Z; Zhang F; Zhou Z; Li Z
J Med Genet; 2021 Oct; 58(10):679-686. PubMed ID: 32900840
[TBL] [Abstract][Full Text] [Related]
6. Analysis of copy number variation in men with non-obstructive azoospermia.
Wyrwoll MJ; Wabschke R; Röpke A; Wöste M; Ruckert C; Perrey S; Rotte N; Hardy J; Astica L; Lupiáñez DG; Wistuba J; Westernströer B; Schlatt S; Berman AJ; Müller AM; Kliesch S; Yatsenko AN; Tüttelmann F; Friedrich C
Andrology; 2022 Nov; 10(8):1593-1604. PubMed ID: 36041235
[TBL] [Abstract][Full Text] [Related]
7. Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest.
van der Bijl N; Röpke A; Biswas U; Wöste M; Jessberger R; Kliesch S; Friedrich C; Tüttelmann F
Hum Reprod; 2019 Nov; 34(11):2112-2119. PubMed ID: 31682730
[TBL] [Abstract][Full Text] [Related]
8. The second mutation of SYCE1 gene associated with autosomal recessive nonobstructive azoospermia.
Pashaei M; Rahimi Bidgoli MM; Zare-Abdollahi D; Najmabadi H; Haji-Seyed-Javadi R; Fatehi F; Alavi A
J Assist Reprod Genet; 2020 Feb; 37(2):451-458. PubMed ID: 31916078
[TBL] [Abstract][Full Text] [Related]
9. Novel bi-allelic variants in KASH5 are associated with meiotic arrest and non-obstructive azoospermia.
Yang C; Lin X; Ji Z; Huang Y; Zhang L; Luo J; Chen H; Li P; Tian R; Zhi E; Hong Y; Zhou Z; Zhang F; Li Z; Yao C
Mol Hum Reprod; 2022 Jun; 28(7):. PubMed ID: 35674372
[TBL] [Abstract][Full Text] [Related]
10. Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia.
Tang D; Li K; Geng H; Xu C; Lv M; Gao Y; Wang G; Yu H; Shao Z; Shen Q; Jiang H; Zhang X; He X; Cao Y
Reprod Biol Endocrinol; 2022 Apr; 20(1):63. PubMed ID: 35366911
[TBL] [Abstract][Full Text] [Related]
11. A biallelic loss of function variant in HORMAD1 within a large consanguineous Turkish family is associated with spermatogenic arrest.
Okutman O; Boivin M; Muller J; Charlet-Berguerand N; Viville S
Hum Reprod; 2023 Feb; 38(2):306-314. PubMed ID: 36524333
[TBL] [Abstract][Full Text] [Related]
12. A homozygous frameshift variant in SYCP2 caused meiotic arrest and non-obstructive azoospermia.
Xu J; Sun Y; Zhang Y; Ou N; Bai H; Zhao J; Xu S; Luo J; Han S; Li P; Tian R; Zhi E; Huang Y; Zhang J; Liu G; Li Z; Yao C
Clin Genet; 2023 Nov; 104(5):577-581. PubMed ID: 37337432
[TBL] [Abstract][Full Text] [Related]
13.
He WB; Tu CF; Liu Q; Meng LL; Yuan SM; Luo AX; He FS; Shen J; Li W; Du J; Zhong CG; Lu GX; Lin G; Fan LQ; Tan YQ
J Med Genet; 2018 Mar; 55(3):198-204. PubMed ID: 29331980
[TBL] [Abstract][Full Text] [Related]
14. Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia.
Tang D; Lv M; Gao Y; Cheng H; Li K; Xu C; Geng H; Li G; Shen Q; Wang C; He X; Cao Y
Reprod Biol Endocrinol; 2021 Aug; 19(1):129. PubMed ID: 34429122
[TBL] [Abstract][Full Text] [Related]
15. Systematic molecular analyses for 115 karyotypically normal men with isolated non-obstructive azoospermia.
Muranishi Y; Kobori Y; Katoh-Fukui Y; Tamaoka S; Hattori A; Osaka A; Okada H; Nakabayashi K; Hata K; Kawai T; Ogata-Kawata H; Iwahata T; Saito K; Kon M; Shinohara N; Fukami M
Hum Reprod; 2024 May; 39(5):1131-1140. PubMed ID: 38511217
[TBL] [Abstract][Full Text] [Related]
16. Variations of C14ORF39 and SYCE1 Identified in Idiopathic Premature Ovarian Insufficiency and Nonobstructive Azoospermia.
Hou D; Yao C; Xu B; Luo W; Ke H; Li Z; Qin Y; Guo T
J Clin Endocrinol Metab; 2022 Feb; 107(3):724-734. PubMed ID: 34718620
[TBL] [Abstract][Full Text] [Related]
17. Homozygous mutations in C14orf39/SIX6OS1 cause non-obstructive azoospermia and premature ovarian insufficiency in humans.
Fan S; Jiao Y; Khan R; Jiang X; Javed AR; Ali A; Zhang H; Zhou J; Naeem M; Murtaza G; Li Y; Yang G; Zaman Q; Zubair M; Guan H; Zhang X; Ma H; Jiang H; Ali H; Dil S; Shah W; Ahmad N; Zhang Y; Shi Q
Am J Hum Genet; 2021 Feb; 108(2):324-336. PubMed ID: 33508233
[TBL] [Abstract][Full Text] [Related]
18. Biallelic HFM1 variants cause non-obstructive azoospermia with meiotic arrest in humans by impairing crossover formation to varying degrees.
Xie X; Murtaza G; Li Y; Zhou J; Ye J; Khan R; Jiang L; Khan I; Zubair M; Yin H; Jiang H; Liu W; Shi B; Hou X; Gong C; Fan S; Wang Y; Jiang X; Zhang Y; Zhang H; Ma H; Shi Q
Hum Reprod; 2022 Jun; 37(7):1664-1677. PubMed ID: 35526155
[TBL] [Abstract][Full Text] [Related]
19. Whole-exome sequencing of consanguineous families with infertile men and women identifies homologous mutations in SPATA22 and MEIOB.
Wu Y; Li Y; Murtaza G; Zhou J; Jiao Y; Gong C; Hu C; Han Q; Zhang H; Zhang Y; Shi B; Ma H; Jiang X; Shi Q
Hum Reprod; 2021 Sep; 36(10):2793-2804. PubMed ID: 34392356
[TBL] [Abstract][Full Text] [Related]
20. A recurrent ZSWIM7 mutation causes male infertility resulting from decreased meiotic recombination.
Li Y; Wu Y; Zhou J; Zhang H; Zhang Y; Ma H; Jiang X; Shi Q
Hum Reprod; 2021 Apr; 36(5):1436-1445. PubMed ID: 33713115
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]